Kinney R M, Esposito J J, Johnson B J, Roehrig J T, Mathews J H, Barrett A D, Trent D W
Division of Vector-Borne Viral Diseases, Centers for Disease Control, Fort Collins, Colorado.
J Gen Virol. 1988 Dec;69 ( Pt 12):3005-13. doi: 10.1099/0022-1317-69-12-3005.
cDNA molecules encoding the structural proteins of the virulent Trinidad donkey and the TC-83 vaccine strains of Venezuelan equine encephalitis (VEE) virus were inserted under control of the vaccinia virus 7.5K promoter into the thymidine kinase gene of vaccinia virus. Synthesis of the capsid protein and glycoproteins E2 and E1 of VEE virus was demonstrated by immunoblotting of lysates of CV-1 cells infected with recombinant vaccinia/VEE viruses. VEE glycoproteins were detected in recombinant virus-infected cells by fluorescent antibody (FA) analysis performed with a panel of VEE-specific monoclonal antibodies. Seven E2-specific epitopes and two of four E1-specific epitopes were demonstrated by FA.
将编码委内瑞拉马脑炎(VEE)病毒强毒株特立尼达驴株和TC - 83疫苗株结构蛋白的cDNA分子,在痘苗病毒7.5K启动子的控制下,插入痘苗病毒的胸苷激酶基因。通过对感染重组痘苗/VEE病毒的CV - 1细胞裂解物进行免疫印迹,证实了VEE病毒衣壳蛋白以及糖蛋白E2和E1的合成。用一组VEE特异性单克隆抗体进行荧光抗体(FA)分析,在重组病毒感染的细胞中检测到了VEE糖蛋白。通过FA证实了七个E2特异性表位和四个E1特异性表位中的两个。